NCAM1, neural cell adhesion molecule 1, 4684

N. diseases: 445; N. variants: 34
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1816537
rs1816537 		11 113097929 intron variant A/C snv 0.50
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 3 2015 2018
dbSNP: rs3802850
rs3802850 		11 113041796 intron variant A/C snv 0.45
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs643830
rs643830 		11 113235826 intron variant A/C snv 1.5E-02
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs643830
rs643830 		11 113235826 intron variant A/C snv 1.5E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2155292
rs2155292 		11 113040061 intron variant A/G snv 0.45
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs2301228
rs2301228 		1.000 0.040 11 112960736 non coding transcript exon variant A/G snv 8.9E-02
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.010 1.000 1 2014 2014
dbSNP: rs61902492
rs61902492 		11 113121199 intron variant A/G;T snv
CUI: C0037369
Disease: Smoking
Smoking 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs1940700
rs1940700 		11 113032833 intron variant A/T snv 1.3E-02
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1940700
rs1940700 		11 113032833 intron variant A/T snv 1.3E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs782464336
rs782464336 		1.000 0.040 11 113275350 missense variant A/T snv 4.0E-06
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs646558
rs646558 		1.000 0.040 11 113235185 intron variant C/A snv 0.22 0.29
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.010 1.000 1 2007 2007
dbSNP: rs11214475
rs11214475 		11 113073328 intron variant C/A;G;T snv
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs10891483
rs10891483 		11 112967156 intron variant C/G;T snv
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2018 2018
dbSNP: rs11214489
rs11214489 		11 113105212 intron variant C/T snv 0.22
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs12574893
rs12574893 		1.000 0.040 11 113046389 intron variant C/T snv 0.19
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs12574893
rs12574893 		1.000 0.040 11 113046389 intron variant C/T snv 0.19
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs2155645
rs2155645 		11 113042225 intron variant C/T snv 0.25
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs4471463
rs4471463 		1.000 11 113112873 intron variant C/T snv 0.57
CUI: C3160814
Disease: Cannabis use
Cannabis use 		0.700 1.000 1 2016 2016
dbSNP: rs4492854
rs4492854 		1.000 0.080 11 113112812 intron variant C/T snv 0.57
CUI: C0019337
Disease: Heroin Dependence
Heroin Dependence 		Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2013 2013
dbSNP: rs72995548
rs72995548 		1.000 0.040 11 113268199 non coding transcript exon variant C/T snv 3.5E-02
CUI: C0525045
Disease: Mood Disorders
Mood Disorders 		Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs72995548
rs72995548 		1.000 0.040 11 113268199 non coding transcript exon variant C/T snv 3.5E-02
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs10891499
rs10891499 		11 113053392 intron variant G/A snv 0.43
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs1940709
rs1940709 		1.000 0.040 11 112978997 intron variant G/A snv 0.30
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs1940709
rs1940709 		1.000 0.040 11 112978997 intron variant G/A snv 0.30
CUI: C0525045
Disease: Mood Disorders
Mood Disorders 		Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs2155287
rs2155287 		11 112976484 intron variant G/A snv 0.16
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012